Capillary Equilibrium in Porous Materials

1965 ◽  
Vol 5 (01) ◽  
pp. 15-24 ◽  
Author(s):  
Norman R. Morrow ◽  
Colin C. Harris

Abstract The experimental points which describe capillary pressure curves are determined at apparent equilibria which are observed after hydrodynamic flow has ceased. For most systems, the time required to obtain equalization of pressure throughout the discontinuous part of a phase is prohibitive. To permit experimental points to be described as equilibria, a model of capillary behavior is proposed where mass transfer is restricted to bulk fluid flow. Model capillary pressure curves follow if the path described by such points is independent of the rate at which the saturation was changed to attain a capillary pressure point. A modified suction potential technique is used to study cyclic relationships between capillary pressure and moisture content for a porous mass. The time taken to complete an experiment was greatly reduced by using small samples. Introduction Capillary retention of liquid by porous materials has been investigated in the fields of hydrology, soil science, oil reservoir engineering, chemical engineering, soil mechanics, textiles, paper making and building materials. In studies of the immiscible displacement of one fluid by another within a porous bed, drainage columns and suction potential techniques have been used to obtain relationships between pressure deficiency and saturation (Fig. 1). Except where there is no hysteresis of contact angle and the solid is of simple geometry, such as a tube of uniform cross section, there is hysteresis in the relationship between capillary pressure and saturation. The relationship which has received most attention is displacement of fluid from an initially saturated bed (Fig. 1, Curve Ro), the final condition being an irreducible minimum fluid saturation Swr. Imbibition (Fig. 1, Curve A), further desaturation (Fig. 1, Curve R), and intermediate scanning curves have been studied to a lesser but increasing extent. This paper first considers the nature of the experimental points tracing the capillary pressure curves with respect to the modes and rates of mass transfer which are operative during the course of measurement. There are clear indications that the experimental points which describe these curves are obtained at apparent equilibria which are observed when viscous fluid flow has ceased; and any further changes in the fluid distribution are the result of much slower mass transfer processes, such as diffusion. Unless stated otherwise, this discussion applies to a stable packing of equal, smooth, hydrophilic spheres supported by a suction plate with water as the wetting phase and air as the nonwetting phase. SPEJ P. 15ˆ

1999 ◽  
Vol 2 (02) ◽  
pp. 141-148 ◽  
Author(s):  
J.V. Nørgaard ◽  
Dan Olsen ◽  
Jan Reffstrup ◽  
Niels Springer

Summary A new technique for obtaining water-oil capillary pressure curves, based on nuclear magnetic resonance (NMR) imaging of the saturation distribution in flooded cores is presented. In this technique, a steady-state fluid saturation profile is developed by flooding the core at a constant flow rate. At the steady-state situation where the saturation distribution no longer changes, the local pressure difference between the wetting and nonwetting phases represents the capillary pressure. The saturation profile is measured using an NMR technique and for a drainage case, the pressure in the nonwetting phase is calculated numerically. This paper presents the NMR technique and the procedure for calculating the pressure distribution in the sample. Inhomogeneous samples produce irregular saturation profiles, which may be interpreted in terms of variation in permeability, porosity, and capillary pressure. Capillary pressure curves for North Sea chalk obtained by the new technique show good agreement with capillary pressure curves obtained by traditional techniques. Introduction Accurate petrophysical properties of reservoir rock such as capillary pressure, permeability, and relative permeability functions are essential as input for reliable oil in place estimations and for the prediction of the reservoir performance. Traditional methods for capillary pressure measurements are the mercury injection method, the diaphragm method, and the centrifuge method. In the mercury injection method,1 the nonwetting phase is mercury which displaces a gas. The samples are usually evacuated to a low pressure and Hg is then injected in steps allowing for pressure equilibrium at each step, or alternatively Hg is continuously injected. Corresponding data on injected volume of Hg and the injection pressure are recorded. This technique is widely used for measuring capillary pressure functions for low permeability rocks. This is primarily because it is generally believed that pressure equilibrium in each pressure step is readily obtained, while this is normally a problem for other methods where a liquid is the wetting phase. The disadvantage of this technique is the uncertainty in the scaling of the measured data to reservoir fluid data and conditions. In the diaphragm method or porous plate method, the problem concerning the scaling of the measured data is avoided, since this technique allows for the direct use of reservoir fluids. A water saturated sample is placed on a water-wet diaphragm to impose a boundary condition pc=0 to the wetting phase, i.e., the wetting phase is allowed to drain through the outlet end of the sample, at the same time as the nonwetting phase (oil or gas) is impeded. Pressure is added to the nonwetting phase and through a limited number of pressure steps, the capillary pressure curve is recorded. However, an important requirement is that equilibrium is obtained at each pressure step. This is the major problem when the diaphragm method is used on microporous materials. The drainage time may be considerable for each step, e.g., several weeks. In recent studies, thin micropore membranes have been used in an attempt to reduce the experimental time.2 Such a reduction will be less pronounced for low permeability rocks such as chalk since the flow resistance in the core is relatively more important. In the centrifuge method, the amount of liquid produced from the outlet end of the plug sample at a certain spin rate is read directly from a measuring tube during rotation. From the geometry of the centrifuge, the spin rate and the average fluid saturation in the plug, it is possible to calculate the capillary pressure relative to the inlet end of the sample.3 However, a number of assumptions must be made3,4: the sample must be homogeneous and have a well-defined outlet pressure boundary condition, i.e., condition pc=0, and drainage equilibrium must be established at each spin rate. Most of these conditions can only be approximated in practice. For the centrifuge method, the condition of drainage equilibrium may be questionable even for sandstone samples.5 Slobod6 reported that equilibrium had not been attained for a 2 mD sample after 20 hr of spinning. King7 concluded that low permeability rock samples may suffer from very long equilibrium times. After 10 days of spinning in the centrifuge, a Berea sandstone sample of 200 mD had just reached equilibrium. The objective of the development of the method presented here has been to avoid some of the disadvantages of the conventional methods described above. In this method a capillary pressure curve is obtained from a measured saturation profile after flooding the core. A similar experimental procedure was used by Richardson et al.8 to study end effects associated with flooding processes. The technique described here can be used with reservoir fluids. There is no porous plate to increase the flow resistance and the measurement of the capillary pressure function can be an integrated part of traditional flooding processes as performed with, e.g., unsteady-state relative permeability measurements. Only a very limited number of steps are needed, in principle only one step is required, therefore the time requirement for obtaining drainage equilibrium has not proved to be a problem. The technique utilizes the unavoidable end effect present in experiments with low permeability rocks. The capillary pressure function is obtained from the steady-state saturation profile in the core at drainage equilibrium.


2010 ◽  
Vol 13 (03) ◽  
pp. 465-472 ◽  
Author(s):  
Amund Brautaset ◽  
Geir Ersland ◽  
Arne Graue

Summary During waterfloods of six outcrop chalk core-plug samples prepared at various wettabilities, simultaneous local pressures and in-situ fluid saturations were measured. Using high-spatial-resolution magnetic-resonance imaging (MRI) to image fluid saturations and pressure taps with semipermeable disks to measure individual phase pressures allowed calculations of relative permeabilities and the dynamic capillary pressure curves for the imbibition processes. A second objective was to identify individual-fluid saturation changes caused by spontaneous imbibition and viscous displacement to determine the local recovery mechanism and to calculate local recovery factors and in-situ Amott-Harvey indices. The obtained results contribute to improved description and understanding of multiphase-fluid flow in porous media, including in situ measurements of relative permeabilities, dynamic capillary pressure curves, Amott-Harvey Indices, and local oil-recovery mechanisms.


2016 ◽  
Vol 8 (1) ◽  
Author(s):  
István Nemes

AbstractThe main focus of the paper is to introduce a new approach at studying and modelling the relationship of initial water saturation profile and capillarity in water-wet hydrocarbon reservoirs, and describe the available measurement methods and possible applications. As a side track it aims to highlight a set of derivable parameters of mercury capillary curves using the Thomeer-method. Since the widely used mercury capillary pressure curves themselves can lead to over-, or underestimations regarding in-place and technical volumes and misinterpreted reservoir behaviour, the need for a proper capillary curve is reasonable. Combining the results of mercury and centrifuge capillary curves could yield a capillary curve preserving the strengths of both methods, while overcoming their weaknesses. Mercury injection capillary curves were normalized by using the irreducible water saturations derived from centrifuge capillary pressure measurements of the same core plug, and this new, combined capillary curve was applied for engineering calculations in order to make comparisons with other approaches. The most significant benefit of this approach is, that all of the measured data needed for a valid drainage capillary pressure curve represents the very same sample piece.


1963 ◽  
Vol 3 (03) ◽  
pp. 227-235 ◽  
Author(s):  
Robert N. Hoffman

HOFFMAN, ROBERT N., MISSOURI SCHOOL OF MINES, ROLLA, MO. JUNIOR MEMBER AIME Abstract A new technique for determining capillary pressure curves has been developed and tested. The technique differs from previously reported centrifuge techniques in that the centrifuge is slowly accelerated from zero to the maximum desired speed rather than being held constant at particular, progressively higher speeds. An important advantage of this technique over other methods of determining capillary pressure curves is the short time required to obtain the desired amount of data over the chosen pressure range. For example, to obtain 30 data points between 1.2 and 104 psig with a 1.55-in. long, 3/4-in, diameter core using a brine-air system, 6. 6 hours were required with this technique. An equally important development of this paper is an analytic method for the conversion of the data from the centrifuge experiment to capillary pressure curve data. Previously there has been only an approximate conversion available.Although the capillary pressure curves determined by this technique appear to be as accurate as those determined by other techniques, the accuracy could be improved if certain variables, not treated in this experiment, were investigated. Among these are the dynamic distortion of the centrifuge equipment and imperfect initial saturation of the cores. Introduction Pirson defines capillary pressure in a porous medium as "the differential pressure that exists between two fluid phases at their interfaces when they are distributed under static equilibrium within a porous material". Capillary pressure in rocks is known to be a function of fluid saturation, among other things, and a capillary pressure curve is defined for the purposes of this paper as a plot of the capillary pressure-wetting phase saturation relationship for a particular rock sample.Several methods are used for determining capillary pressure curves for small rock cores. Prominent among these are the semi-permeable barrier, mercury injection, and, to a lesser extent, centrifuge methods. The semi-permeable barrier method is currently the most popular. It features simplicity in both execution and the mathematical conversion of the experimental data into a capillary pressure curve. The main disadvantages of the semi-permeable barrier method are the time required - as long as two months - to obtain several points for the curve, and a fairly low maximum pressure before breakthrough of the non- wetting phase into the barrier occurs, for example, about 32 psig for a brine-air system.It is for these reasons that other methods such as the centrifuge method have been introduced. High accelerations and the absence of a barrier result in quicker attainment of saturation equilibrium at a given pressure. However, the centrifuge method involves much more expensive equipment and more difficult procedures and calculations than does the barrier method. The purpose of this investigation has been to improve the equipment and procedures of the centrifuge method and to develop an analytic method for the conversion of the experimental data into a capillary pressure curve.Hassler and Brunner did the original work in the determination of capillary pressure using a centrifuge. In their work the centrifuge speed was increased in a step-wise manner, each speed being held constant until saturation equilibrium was reached in each core. Saturation equilibrium was indicated when the volume of liquid collected in the graduated pipette of the core holder remained constant. According to Hassler and Brunner, equilibrium was reached in "a few minutes to one-half hour or more".In the centrifuge method, as opposed to the barrier method, the fluid saturation of the core is not a constant throughout the length of the core, but varies with the radius of centrifugation. Also, the capillary pressure cannot be read directly but must be calculated from a knowledge of the centrifuge speed and other parameters. SPEJ P. 227^


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